Associate Principal / Principal Scientist (Protein Science)

Posted 2 Days Ago
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Singapore, SGP
In-Office
Senior level
Biotech
The Role
Lead antibody design and engineering for complex formats (bispecifics, multivalent, Fc-fusions, VHH). Drive platform building, troubleshoot expression and manufacturability, supervise staff, integrate AI/computational design with experimental validation, collaborate cross-functionally, support tech transfer, and contribute to IP and scientific communications.
Summary Generated by Built In
About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

Position Overview:
We are seeking a highly motivated and experienced Principal Scientist in Bispecific Antibody Design & Engineering to establish and strengthen Singapore’s role as a center of excellence for complex antibody design and molecular engineering. In this role, you will serve as a functional leader in molecular design, format selection and recommendation, and engineering strategy while enabling improved expression, developability, and manufacturability. Additionally, you will play a key role in client-facing projects, ensuring seamless collaboration and delivery of high-quality biologics solutions. This position requires a blend of platform building, leadership skills, and the ability to build cross effectively.


Key Responsibilities:

Biologics Production Leadership:

  • Develop, triage, implement, and troubleshoot innovative strategies for the design and engineering of complex antibody formats (bispecifics, multivalent, Fc-fusions, VHH). to achieve high yields, purity, and functionality.
  • Design and manage a portfolio of projects to provide data-driven, structure-function insights to improve expression, stability, and manufacturability.
  • Oversee a team of research associates and/or biotechnologists, providing technical guidance and fostering a culture of excellence in protein science methodologies.

Cross-Functional Collaboration:

  • Collaborate with cross-functional and cross-cultural teams to support the development of biologics, with a focus on evaluate and translate new technologies into production-ready solutions.
  • Periodically review internal and external advancements in:
    • Antibody formats and engineering strategies
    • Upstream and downstream integration impacts driven by molecule design
  • Assess readiness of new technologies for tech transfer, including:
    • Fit-for-purpose application across different molecule classes
    • Scalability and reproducibility
    • Impact on quality attributes (aggregation, mispairing, heterogeneity)
    • Act as a scientific bridge between R&D innovation and operational deployment, ensuring:
      1. New platforms are not only scientifically sound but also translatable to production workflows
      2. Design decisions are aligned with manufacturing realities
    • Partner with internal stakeholders (e.g., Quality Assurance, Process Development, and Manufacturing) to ensure alignment and efficiency in biologics production workflows.

Develop design-for-manufacturability strategies and internal guidelines:

  • Develop and integrate AI-assisted design-for-manufacturability frameworks, leveraging internal datasets and external computational tools (e.g., structure prediction, developability scoring) to proactively identify and mitigate risks such as aggregation, mispairing, and low expression in complex antibody formats.
  • Lead or support AI-enabled design and innovation initiatives (internal and external partnerships, including governmental or consortium projects) by translating computational design outputs into experimentally validated constructs, and ensuring alignment between in silico design predictions and real-world expression, quality, and manufacturability outcomes.

Innovation & Intellectual Property:

  • Generate novel ideas and contribute to the company’s intellectual property portfolio by drafting scientific papers, filing patents and reporting innovations in scientific forums.
  • Contribute to the development of scientific publications, conference presentations, and webinars to showcase innovative findings and advancements.
  • Prepare and review technical reports and documentation to internal and external stakeholders.

 

Qualifications and Preferred Skills:

  • Ph.D., in Biochemistry, Molecular Biology, Cell Biology, Structural Biology, Bioengineering or a related field.
  • At least 5 years of experience in antibody design, protein expression, and purification, preferably in an industrial setting.
  • Strong expertise in bispecific design and troubleshooting expression challenges.
  • A demonstrated record of success with protein engineering for enhanced protein expression or properties.
  • Experience with the biophysical characterization of proteins and the assessment of protein-protein interactions.
  • Familiarity with automation and high-throughput techniques for protein expression and purification.
  • Strong analytical and problem-solving skills, with a wide ranging experience in analytical techniques such as SPR, and mass spectrometry.
  • Excellent written and verbal English communication skills, with a track record of scientific publications, presentations, and conferences.

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

 

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform. 

Skills Required

  • Ph.D. in Biochemistry, Molecular Biology, Cell Biology, Structural Biology, Bioengineering or related field.
  • At least 5 years of experience in antibody design, protein expression, and purification.
  • Experience in an industrial biotechnology or biopharmaceutical setting (preferred).
  • Strong expertise in bispecific antibody design and troubleshooting expression challenges.
  • Demonstrated success in protein engineering to improve expression, stability, or developability.
  • Experience with biophysical characterization and assessment of protein-protein interactions (e.g., SPR, mass spectrometry).
  • Familiarity with automation and high-throughput techniques for protein expression and purification.
  • Experience developing or integrating AI-assisted design, structure prediction, and developability scoring into experimental workflows.
  • Experience leading or overseeing research associates/biotechnologists and managing project portfolios.
  • Excellent written and verbal English communication skills with a track record of scientific publications and presentations.
  • Experience with patent filing or contributing to intellectual property (preferred).

GenScript Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about GenScript and has not been reviewed or approved by GenScript.

  • Healthcare Strength Feedback suggests medical coverage is solid, with mentions of comprehensive health plans and employer HSA support in some options. Company communications also emphasize robust health benefits alongside wellbeing and training initiatives.
  • Leave & Time Off Breadth Feedback suggests a range of paid time off types, including vacation, sick time, company holidays, and additional leave categories. Some roles reference flexible vacation arrangements that broaden usable time off.
  • Retirement Support Feedback suggests retirement offerings include a 401(k) with company match in certain postings. This provides a longer-term savings component within total rewards.

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The Company
HQ: Piscataway, NJ
883 Employees
Year Founded: 2002

What We Do

Founded in 2002 and listed on the Hong Kong Stock Exchange in 2015, GenScript has an established global presence across Greater China, North America, the EU, and Asia Pacific. Today, over 300,000 customers from over 160 countries and regions worldwide have used GenScript’s premier, convenient, and reliable products and services. GenScript currently has over 5,000 employees globally, 33% holding master’s and/or Ph.D. degrees. In addition, GenScript has a number of leading commercial technologies developed in the fields of synthetic biology, immunotherapy, antibody design, chemical synthesis, and bioinformatics, including more than 100 patents and over 270 patent applications. As of June 2022, GenScript's products and services have been cited by 74,700 scientific papers worldwide. GenScript is committed to striving toward its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

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